Impact of Daridorexant on Sleep, Daytime Alertness, and Smoking

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-55
SponsorLegacy Health System

About this trial

Tobacco use is the leading cause of preventable death in the U.S., with 480,000 deaths per year and 7.7 million deaths globally. A major clinical symptom associated with abstinence from both licit and illicit drugs is insomnia, which is a clinically verified, major risk factor for relapse. Roughly half of the 40 million smokers in the U.S. attempt to quit annually, with very low rates of success. One major hurdle is poor sleep quality during abstinence. Compounding the problem is that some pharmaceuticals to help reduce smoking can increase insomnia. Poor sleep is recognized as a major impediment to maintaining abstinence from several drugs of abuse, including nicotine. Blockers of orexin have recently been proposed as a promising therapy for smoking cessation. Insomnia has been reported in up to 40% of smokers, and 80% report regular sleep disturbances, which can be amplified during abstinence. A new orexin blocker, daridorexant, was FDA approved within the past two years for the treatment of insomnia, and while it has been tested in healthy individuals with insomnia, it has not been tested in smokers, who suffer from insomnia, particularly during the withdrawal phase when trying to quit. Daridorexant has an improved profile of beneficial effects for those with insomnia, the most notable advantage being its shorter duration of action that promotes daytime alertness, which is problematic for both active smokers and smokers during withdrawal. Poor sleep leads to daytime sleepiness, which often leads to smoking to maintain alertness.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult participants who are cigarette smokers, 18-55 years of age.

Smokers: greater than 10 cigarettes/day.

Smoking for 1 year or longer.

Willingness to try to reduce or stay abstinent from cigarettes, smoking cessation aides (including nicotine gum or patches), smokeless tobacco, or electronic cigarettes for 3 weeks during the study.

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Daridorexant 50 mg

    Drug

    Active daridorexant vs placebo comparator in smokers with insomnia

  • Placebo

    Other intervention

    Placebo in Smokers

Treatment groups

44 Participants
are divided into 2 treatment groups
Group A: TreatmentActive comparator 1 intervention
Group B: No treatmentPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Sleep Quality

Sleep device to assess: latency to sleep, number of awakenings during the night, and sleep stages.

Time frame
2 days + 3 weeks study: 2 days to assess sleep prior to taking daridorexant followed by 3 weeks of daily daridorexant administration.
2

Daytime alertness

Assess daytime alertness using a 5 min psychomotor vigilance task. Higher score indicates lower alertness.

Time frame
Assessed 3 times per day (morning, midday, evening), 3 times per week for 3 weeks.
3

Insomnia Severity Index

Assesses extent of insomnia. Range is 0-28. Higher score indicates high level of insomnia.

Time frame
Assess at prescreening and on last day of the study (3 weeks and 2 days)
4

Sleep Quality-sleep diary

Daily sleep diary to assess self-reported sleep

Time frame
Assessed 2 days prior to taking daridorexant and daily for 3 weeks during daily daridorexant administration.

Secondary outcomes

1

Fagerstrom

Assesses extent of nicotine dependence. Range is 0-10. Higher score indicates higher dependence.

Time frame
Measure at pre-screening and at the end of each week for 3 weeks.
2

Smoking History and Habits

Must smoke 10 or more cigarettes per day.

Time frame
Measure at pre-screening.
3

Minnesota Scale Withdrawal from Nicotine

Assesses nicotine withdrawal symptoms over last 24 hr. Range is 0-60, higher score indicating higher withdrawal signs/symptoms.

Time frame
2 days before beginning study medication, end of day on days 3, 5, 7 of weeks 1, 2, and 3.
4

QSU Brief Smoking Desire

Assesses desire to smoke. Range 7-49. Higher score indicates higher craving to smoke.

Time frame
End of day on days 3, 5, 7 of weeks 1, 2, and 3.

Other outcomes

1

Morningness/Eveningness questionnaire

Scores range from 16-83, with higher score indicating morning type and lower score evening type.

Time frame
2 days before beginning study medication
2

GAD-67 Anxiety

Assesses anxiety levels over last 2 weeks. Range is 0-21, higher score indicating higher anxiety.

Time frame
2 days before beginning study medication and last day of the study (3 weeks, 2 days).
3

Patient Health Questionnaire 9 (PHQ 9 Depression)

Assesses depression levels. Range is 1-27, higher score indicating higher depression.

Time frame
2 days before beginning study medication and last day of the study (3 weeks, 2 days).
4

Readiness to Quit

Readiness to quit tobacco. Scale is 1-10, with higher score indicating more important to quit.

Time frame
2 days before beginning study medication and on last day of study (3 weeks, 2 days).

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Legacy Health System

Lead sponsor

Washington State University

Collaborator

This trial is not recruiting at the moment. You can still explore other options: